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2981 metabolic genes  (Addgene inc)


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    Addgene inc 2981 metabolic genes
    ( A ) Schematic illustration <t>of</t> <t>CRISPR-Cas9</t> screen workflow. ( B ) Top 10 negatively selected genes ranked by robust rank aggregation (RRA) score in 10 Gy–irradiated group compared to the control. ( C ) Manhattan plot of the entire <t>2981</t> metabolic genes by log 10 P value. The top 10 negatively selected genes are highlighted. ( D ) Schematic illustration of the function of LIPT1, LIAS, DLD, and PDHX, the four top hits involved in lipoylation. ( E ) Pathway analysis of the 10 most significantly depleted metabolic pathways by Gene Ontology classification in 10 Gy–irradiated cells compared to the nonirradiated cells. ( F ) Immunoblots of total and lipoylated PDH and α-KGDH subunits (DLAT and DLST, respectively). Glyceraldehyde-3-phosphate dehydrogenase (GAPDH), DLAT, and DLST were blotted as loading controls. ( G ) Clonogenic assay of indicated cell lines after 2, 4, 6, and 8 Gy IR. The surviving fraction was normalized to the corresponding sham control, and survival curves were fitted using the linear-quadratic model.
    2981 Metabolic Genes, supplied by Addgene inc, used in various techniques. Bioz Stars score: 93/100, based on 27 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/2981+metabolic+genes/Human+CRISPR+Metabolic+Gene+Knockout+Library+(Pooled+Library+%23110066)/pmc11900879-218-10-13
    Average 93 stars, based on 27 article reviews
    2981 metabolic genes - by Bioz Stars, 2026-09
    93/100 stars

    Images

    1) Product Images from "Lipoylation inhibition enhances radiation control of lung cancer by suppressing homologous recombination DNA damage repair"

    Article Title: Lipoylation inhibition enhances radiation control of lung cancer by suppressing homologous recombination DNA damage repair

    Journal: Science Advances

    doi: 10.1126/sciadv.adt1241

    ( A ) Schematic illustration of CRISPR-Cas9 screen workflow. ( B ) Top 10 negatively selected genes ranked by robust rank aggregation (RRA) score in 10 Gy–irradiated group compared to the control. ( C ) Manhattan plot of the entire 2981 metabolic genes by log 10 P value. The top 10 negatively selected genes are highlighted. ( D ) Schematic illustration of the function of LIPT1, LIAS, DLD, and PDHX, the four top hits involved in lipoylation. ( E ) Pathway analysis of the 10 most significantly depleted metabolic pathways by Gene Ontology classification in 10 Gy–irradiated cells compared to the nonirradiated cells. ( F ) Immunoblots of total and lipoylated PDH and α-KGDH subunits (DLAT and DLST, respectively). Glyceraldehyde-3-phosphate dehydrogenase (GAPDH), DLAT, and DLST were blotted as loading controls. ( G ) Clonogenic assay of indicated cell lines after 2, 4, 6, and 8 Gy IR. The surviving fraction was normalized to the corresponding sham control, and survival curves were fitted using the linear-quadratic model.
    Figure Legend Snippet: ( A ) Schematic illustration of CRISPR-Cas9 screen workflow. ( B ) Top 10 negatively selected genes ranked by robust rank aggregation (RRA) score in 10 Gy–irradiated group compared to the control. ( C ) Manhattan plot of the entire 2981 metabolic genes by log 10 P value. The top 10 negatively selected genes are highlighted. ( D ) Schematic illustration of the function of LIPT1, LIAS, DLD, and PDHX, the four top hits involved in lipoylation. ( E ) Pathway analysis of the 10 most significantly depleted metabolic pathways by Gene Ontology classification in 10 Gy–irradiated cells compared to the nonirradiated cells. ( F ) Immunoblots of total and lipoylated PDH and α-KGDH subunits (DLAT and DLST, respectively). Glyceraldehyde-3-phosphate dehydrogenase (GAPDH), DLAT, and DLST were blotted as loading controls. ( G ) Clonogenic assay of indicated cell lines after 2, 4, 6, and 8 Gy IR. The surviving fraction was normalized to the corresponding sham control, and survival curves were fitted using the linear-quadratic model.

    Techniques Used: CRISPR, Irradiation, Control, Western Blot, Clonogenic Assay

    Related Articles

    CRISPR:

    Article Title: Lipoylation inhibition enhances radiation control of lung cancer by suppressing homologous recombination DNA damage repair.
    Article Snippet: .. The human CRISPR knockout pooled library was designed to target 2981 metabolic genes (Addgene, #110066) (71) and synthesized as a pool of lentiviral vectors containing unique gRNA sequences (70). ..

    Article Title: Lipoylation inhibition enhances radiation control of lung cancer by suppressing homologous recombination DNA damage repair
    Article Snippet: .. The human CRISPR knockout pooled library was designed to target 2981 metabolic genes (Addgene, #110066) ( ) and synthesized as a pool of lentiviral vectors containing unique gRNA sequences ( ). ..

    Knock-Out:

    Article Title: Lipoylation inhibition enhances radiation control of lung cancer by suppressing homologous recombination DNA damage repair.
    Article Snippet: .. The human CRISPR knockout pooled library was designed to target 2981 metabolic genes (Addgene, #110066) (71) and synthesized as a pool of lentiviral vectors containing unique gRNA sequences (70). ..

    Article Title: Lipoylation inhibition enhances radiation control of lung cancer by suppressing homologous recombination DNA damage repair
    Article Snippet: .. The human CRISPR knockout pooled library was designed to target 2981 metabolic genes (Addgene, #110066) ( ) and synthesized as a pool of lentiviral vectors containing unique gRNA sequences ( ). ..

    Synthesized:

    Article Title: Lipoylation inhibition enhances radiation control of lung cancer by suppressing homologous recombination DNA damage repair.
    Article Snippet: .. The human CRISPR knockout pooled library was designed to target 2981 metabolic genes (Addgene, #110066) (71) and synthesized as a pool of lentiviral vectors containing unique gRNA sequences (70). ..

    Article Title: Lipoylation inhibition enhances radiation control of lung cancer by suppressing homologous recombination DNA damage repair
    Article Snippet: .. The human CRISPR knockout pooled library was designed to target 2981 metabolic genes (Addgene, #110066) ( ) and synthesized as a pool of lentiviral vectors containing unique gRNA sequences ( ). ..



    Similar Products

    2981 metabolic genes  (Addgene inc)
    93
    Addgene inc 2981 metabolic genes
    ( A ) Schematic illustration <t>of</t> <t>CRISPR-Cas9</t> screen workflow. ( B ) Top 10 negatively selected genes ranked by robust rank aggregation (RRA) score in 10 Gy–irradiated group compared to the control. ( C ) Manhattan plot of the entire <t>2981</t> metabolic genes by log 10 P value. The top 10 negatively selected genes are highlighted. ( D ) Schematic illustration of the function of LIPT1, LIAS, DLD, and PDHX, the four top hits involved in lipoylation. ( E ) Pathway analysis of the 10 most significantly depleted metabolic pathways by Gene Ontology classification in 10 Gy–irradiated cells compared to the nonirradiated cells. ( F ) Immunoblots of total and lipoylated PDH and α-KGDH subunits (DLAT and DLST, respectively). Glyceraldehyde-3-phosphate dehydrogenase (GAPDH), DLAT, and DLST were blotted as loading controls. ( G ) Clonogenic assay of indicated cell lines after 2, 4, 6, and 8 Gy IR. The surviving fraction was normalized to the corresponding sham control, and survival curves were fitted using the linear-quadratic model.
    2981 Metabolic Genes, supplied by Addgene inc, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/2981+metabolic+genes/Human+CRISPR+Metabolic+Gene+Knockout+Library+(Pooled+Library+%23110066)/pmc11900879-218-10-13
    Average 93 stars, based on 1 article reviews
    2981 metabolic genes - by Bioz Stars, 2026-09
    93/100 stars
    		  Buy from Supplier

    Image Search Results


    ( A ) Schematic illustration of CRISPR-Cas9 screen workflow. ( B ) Top 10 negatively selected genes ranked by robust rank aggregation (RRA) score in 10 Gy–irradiated group compared to the control. ( C ) Manhattan plot of the entire 2981 metabolic genes by log 10 P value. The top 10 negatively selected genes are highlighted. ( D ) Schematic illustration of the function of LIPT1, LIAS, DLD, and PDHX, the four top hits involved in lipoylation. ( E ) Pathway analysis of the 10 most significantly depleted metabolic pathways by Gene Ontology classification in 10 Gy–irradiated cells compared to the nonirradiated cells. ( F ) Immunoblots of total and lipoylated PDH and α-KGDH subunits (DLAT and DLST, respectively). Glyceraldehyde-3-phosphate dehydrogenase (GAPDH), DLAT, and DLST were blotted as loading controls. ( G ) Clonogenic assay of indicated cell lines after 2, 4, 6, and 8 Gy IR. The surviving fraction was normalized to the corresponding sham control, and survival curves were fitted using the linear-quadratic model.

    Journal: Science Advances

    Article Title: Lipoylation inhibition enhances radiation control of lung cancer by suppressing homologous recombination DNA damage repair

    doi: 10.1126/sciadv.adt1241

    Figure Lengend Snippet: ( A ) Schematic illustration of CRISPR-Cas9 screen workflow. ( B ) Top 10 negatively selected genes ranked by robust rank aggregation (RRA) score in 10 Gy–irradiated group compared to the control. ( C ) Manhattan plot of the entire 2981 metabolic genes by log 10 P value. The top 10 negatively selected genes are highlighted. ( D ) Schematic illustration of the function of LIPT1, LIAS, DLD, and PDHX, the four top hits involved in lipoylation. ( E ) Pathway analysis of the 10 most significantly depleted metabolic pathways by Gene Ontology classification in 10 Gy–irradiated cells compared to the nonirradiated cells. ( F ) Immunoblots of total and lipoylated PDH and α-KGDH subunits (DLAT and DLST, respectively). Glyceraldehyde-3-phosphate dehydrogenase (GAPDH), DLAT, and DLST were blotted as loading controls. ( G ) Clonogenic assay of indicated cell lines after 2, 4, 6, and 8 Gy IR. The surviving fraction was normalized to the corresponding sham control, and survival curves were fitted using the linear-quadratic model.

    Article Snippet: The human CRISPR knockout pooled library was designed to target 2981 metabolic genes (Addgene, #110066) ( ) and synthesized as a pool of lentiviral vectors containing unique gRNA sequences ( ).

    Techniques: CRISPR, Irradiation, Control, Western Blot, Clonogenic Assay